Active Ingredient: SULINDAC
Proprietary Name: SULINDAC
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072713
Product Number: 001
Approval Date: Aug 30, 1991
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information